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Albuterol

NDC 59651-334, Albuterol, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-334
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213657
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-334 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ALBUTEROL SULFATE4 mg/1

Pharmacologic classes

Adrenergic beta2-Agonists [MoA]; beta2-Adrenergic Agonist [EPC]

Package NDCNDC-11Package
59651-334-0159651033401100 TABLET in 1 BOTTLE (59651-334-01)
59651-334-0559651033405500 TABLET in 1 BOTTLE (59651-334-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff9b287b-e4a4-4c12-ad2f-6b7d55b20dc6

Use it

Look up 59651-334 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-334 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-334. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.